首页> 外国专利> DIFFERENTIATION METHOD OF BIOVARS AND GENOVARIATIONS OF Yersinia pestis STRAINS OF MAIN SUBSPECIES BY MEANS OF POLYMERASE CHAIN REACTION

DIFFERENTIATION METHOD OF BIOVARS AND GENOVARIATIONS OF Yersinia pestis STRAINS OF MAIN SUBSPECIES BY MEANS OF POLYMERASE CHAIN REACTION

机译:聚合酶链反应法对主要亚种鼠疫耶尔森菌的生物体分化和遗传鉴定方法

摘要

FIELD: biotechnologies.SUBSTANCE: method provides for separation of DNA of the test strain, series performance of a polymerase chain reaction (PCR) with Med24, glpD, pCKF primers on a DNA target and with 1.ANT/1.ORI, 2.ANT/2.MED primers of the following composition: Med24-S GTATTTTGTGTCACCCC Med24-As AATGAGACACCGCCAGT glpD-F1 GGCTAGCCGCCTCAACAAAAACAT glpD-R1 GGTCATACAAGAACAAGCCGGTGC pCKF-S TCCGTGCTCATTGGTTCG pCKF-As AGACTTGGCGAACGTGGT 1.ANT/1.ORI-S CGTTCTGCTCTCTGTTTGTC 1.ANT/1.ORI-As GTAGAGATGTGTTGCCCG 2.ANT/2.MED-S AAGACCTTCGCCACCAGA 2.ANT/2.MED-As CCAGGATTCGCCGATTCA. Differentiation is performed by comparison of availability and sizes of the formed amplified fragments of the test strain with dimensions of fragments of typical strains of ancient (genovariations 0.ANT, 1.ANT, 2.ANT), mediaeval (genovariations 2.MED, 2.MED0) and eastern (genovariation 1.ORI) biovars.EFFECT: invention allows quick and effective separation of strains of plague originator as to their biovar and intrabiovar belonging.1 tbl, 3 ex
机译:领域:生物技术。目的:该方法可分离测试菌株的DNA,并在DNA靶标上使用Med24,glpD,pCKF引物并使用1.ANT / 1.ORI,2.进行聚合酶链反应(PCR)的系列性能。具有以下组成的ANT / 2.MED引物:Med24-S GTATTTTGTGTCACCCC Med24-As AATGAGACACCGCCAGT glpD-F1 GGCTAGCCGCCTCAACAAAAACAT glpD-R1 GGTCATACAAGAACAAGCCGGTGC pCKF-S TCCGTGCTCTCGGTTCG pCKF-As 1。 .ORI-As GTAGAGATGTGTTGCCCG 2.ANT / 2.MED-S AAGACCTTCGCCACCAGA 2.ANT / 2.MED-As CCAGGATTCGCCGATTCA。通过比较测试菌株形成的扩增片段的可用性和大小与古代(遗传变异0.ANT,1.ANT,2.ANT),中世纪(遗传变异2.MED,2)典型菌株片段的大小进行区分MED0)和东部(遗传变异1.ORI)生物变种。效果:本发明可以快速有效地分离鼠疫起源生物体和生物体内变种的菌株。1 tbl,3 ex

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